Evaluation of α- and β-pinene degradation in the detailed tropospheric chemistry mechanism,MCM v3.1, using environmental chamber data   总被引：1，自引：0，他引：1  

P. G. Pinho  C. A. Pio  W. P. L. Carter  M. E. Jenkin 《Journal of Atmospheric Chemistry》2007,57(2):171-202

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Evaluation of Electro-Oxidation of Textile Effluent Using Response Surface Methods     

R. Saravanathamizhan  N. Mohan  N. Balasubramanian  V. Ramamurthi  C. Ahmed Basha 《洁净——土壤、空气、水》2007,35(4):355-361

In the present investigation, treatment of textile effluent using an electrochemical technique was designed and analyzed using the Box-Behnken method. The influence of individual parameters on electro-oxidation of textile effluent has been critically examined using the response surface method (RSM), and a quadratic model for chemical oxygen demand (COD) reduction has been developed. It has been observed from the present analysis that the predicted values are in good agreement with experimental data with a correlation coefficient of 0.945.  相似文献   

A comparative mineralogical and geochemical study of sulfide mine tailings at two sites in New Mexico, USA   总被引：5，自引：0，他引：5  

Michelle P. Boulet  A. C. L. Larocque 《Environmental Geology》1998,33(2-3):130-142

A comparative study of sulfide mine tailings from two sites near Silver City in southwest New Mexico has shown the need for environmental monitoring in a geological context. The Cyprus-Piños Altos and Cleveland deposits consist of Cu and Zn skarn mineralization in the Piños Altos Mountains of New Mexico. Primary ore minerals in both deposits include chalcopyrite, sphalerite, and galena. The Cyprus-Piños Altos Mine ceased operation in 1995 and the Cleveland Mill closed in 1950. The deposits have similar mineralogical characteristics; however, the tailings are different in terms of age, degree of oxidation and method of disposal. The Cyprus-Piños Altos tailings (CPAT) are stored in a lined, bermed impoundment. They are dominantly water-saturated and exhibit no secondary-phase formation. The grains are not cemented and show no evidence of primary-mineral dissolution. The geochemical data show a predominantly primary signature. The tailings pond water is neutral to slightly alkaline (pH?from 7 to 8.3), partly as a result of processing methods. The Cleveland mill tailings (CMT) were deposited in a valley at the headwaters of an ephemeral stream. They are highly oxidized and differentially cemented. They have undergone numerous wet/dry cycles resulting in extensive oxidation. Secondary minerals predominate, and consist mainly of jarosite, goethite, hematite, and Fe-oxyhydroxides and -oxyhydroxysulfates. The pH of the stream draining the CMT is as high as 2.15. Maximum metal contents in the stream immediately downstream from the tailings are 5305?ppm Zn, 454?ppm Cu, 1.16?ppm Pb, 17.5?ppm Cd, 1.4?ppm As, and 0.01?ppm Hg.  相似文献   

西藏玉龙铜矿床次生氧化富集作用机制   总被引：8，自引：0，他引：8  

陈建平  王成善 《地质学报》1998,72(2):153-161

作文阐述了西藏玉龙铜矿床成矿过程中的“沉积初步富集期”和“西藏玉龙铜矿床次生氧化成矿作用模式”,这不仅对指导当前生产具有重要的现实意义,而且为在玉龙铜矿带进一步找矿共作劈了新的方向。  相似文献   

松辽盆地西南部层间氧化带砂岩型铀矿找矿方向   总被引：16，自引：1，他引：15  

赵忠华  刘广传  崔长远 《矿物岩石地球化学通报》1998,(3)

松辽盆地西南部层间氧化带砂岩型铀矿找矿方向赵忠华刘广传崔长远（核工业东北地质局２４０研究所,沈阳１１００３２）关键词开鲁盆地层间氧化带砂岩型铀矿找矿松辽盆地西南部系指内蒙古自治区哲里木盟及昭乌达盟所辖地区,西临大兴安岭,南依辽西山地,面积约６００００...  相似文献   

Fast Oxidation Reaction of Nitrite by Dissolved Oxygen in the Freezing Process in the Tropospheric Aqueous Phase     

Norimichi Takenaka  Tohru Daimon  Akihiro Ueda  Keiichi Sato  Masaru Kitano  Hiroshi Bandow  Yasuaki Maeda 《Journal of Atmospheric Chemistry》1998,29(2):135-150

Nitrite oxidation in the tropospheric aqueous phase by freezing was evaluated by freezing a field sample. Nitrite oxidation by dissolved oxygen in the freezing process is much faster than by other oxidation processes, such as reactions with ozone, hydrogen peroxide or dissolved oxygen in an aqueous solution at pHs 3 to –6. At pH 4.5 and 25°C, the lifetime of nitrite in the aqueous phase is ca. 1 hr in oxidation by ozone (6×10^-10 mol dm^-3), ca. 10 hr in oxidation by H₂O₂ (2×10^-4 mol dm^-3), and 7.5 hr (Fischer and Warneck, 1996) in photodissociation at midday in summer. Under the same conditions at a temperature below 0°C, the lifetime of nitrite in the freezing process is estimated as ca. 2 sec when the droplets are frozen within a second. The reaction by freezing is affected by the presence of salts, such as NaCl or KCl, or orgnaic compounds, such as methanol or acetone. The results of freezing a field rain or fog sample showed that nitrite oxidation proceeds below pH 6, and the conversion ratio of nitrate from nitrite increases with decreasing pH. The oxidation of nitrite by freezing was also observed in freezing fog particles generated by an ultrasonic humidifier. The ratios of the concentrations of ions in the winter sample to those in the summer sample (or those in the fog sample) were almost the same values. However, the concentration of nitrite in the winter sample was lower than that estimated by the ratios of other ions. From the present study, it seems that the freezing process plays an important role in the nitrite sink process in the tropospheric aqueous phase.  相似文献   

A Three-Dimensional Global Model Study of Carbonyl Sulfide in the Troposphere and the Lower Stratosphere   总被引：4，自引：0，他引：4  

Erik Kjellström 《Journal of Atmospheric Chemistry》1998,29(2):151-177

Global distributions of carbonyl sulfide and carbon disulfide have been calculated with a three-dimensional global model of the atmospheric general circulation (ECHAM). The model calculates a global sink strength for carbonyl sulfide of 0.3 Tg S yr^-1, with vegetation uptake being the largest sink. With this sink strength, the sources have to be close to the lower limit of the present estimate in the literature. The calculated mixing ratios are higher in the Southern Hemisphere than in the Northern Hemisphere. This interhemispheric gradient is the opposite of what is observed demonstrating that the present knowledge of the distribution of sinks and sources is not fully adequate. The model calculations support the idea that the open oceans could act as a net sink of carbonyl sulfide. The calculated stratospheric photolysis of carbonyl sulfide constitutes about 4% of the total sink of carbonyl sulfide. A stratospheric production of sulfate from carbonyl sulfide of 0.013 Tg S yr^-1 is obtained, which is 3 to 12 times less than what is needed to maintain the stratospheric sulfate aerosol layer. Although these results are associated with uncertainties, due to the low upper boundary and coarse vertical resolution of the model, they support recent findings of a low stratospheric production of sulfate from carbonyl sulfide. Instead, sulfur dioxide transported from the troposphere is calculated to be the most important precursor for the stratospheric sulfate aerosol layer.  相似文献   

Model Simulations on the Variability of Particulate MSA to Non-Sea-Salt Sulfate Ratio in the Marine Environment     

Veli-Matti Kerminen  Risto E. Hillamo  Anthony S. Wexler 《Journal of Atmospheric Chemistry》1998,30(3):345-370

A box model was constructed to investigate connections between the particulate MSA to non-sea-salt sulfate ratio, R, and DMS chemistry in a clean marine boundary layer. The simulations demonstrated that R varies widely with particle size, which must be taken into account when interpreting field measurements or comparing them with each other. In addition to DMS gas-phase chemistry, R in the submicron size range was shown to be sensitive to the factors dictating sulfate production via cloud processing, to the removal of SO₂ from the boundary layer by dry deposition and sea-salt oxidation, to the entrainment of SO₂ from the free troposphere, to the relative concentration of sub- and supermicron particles, and to meteorology. Three potential explanations for the increase of R toward high-latitudes during the summer were found: larger MSA yields from DMS oxidation at high latitudes, larger DMSO yields from DMS oxidation followed by the conversion of DMSO to MSA at high latitudes, or lower ambient H₂O₂ concentrations at high latitudes leading to less efficient sulfate production in clouds. Possible reasons for the large seasonal amplitude of R at mid and high latitudes include seasonal changes in the partitioning of DMS oxidation to the OH and NO₃ initiated pathways, seasonal changes in the concentration of species participating the DMS-OH reaction pathway, or the existence of a SO₂ source other than DMS oxidation in the marine boundary layer. Even small anthropogenic perturbations were shown to have a potential to alter the MSA to non-sea-salt sulfate ratio.  相似文献   

南海东沙东北部甲烷缺氧氧化作用的生物标志化合物及其碳同位素组成   总被引：5，自引：0，他引：5  

于晓果  韩喜球  李宏亮  金肖兵  龚建明  ErwinSUESS  黄永样  吴能友  苏新 《海洋学报》2008,30(3):77-84

南海东沙东北部碳酸盐岩和泥质沉积物中的生物标志化合物组合及其碳同位素组成分析表明,研究区内甲烷缺氧氧化作用(anaerobic oxidation of methane-AOM)发育.研究区内碳酸盐岩中含丰富的AOM标志化合物,2,6,11,15-四甲基十六烷(Crocetane-Cr.)、2,6,10,15,19-五甲基番茄烷(Pentamethylicosane-PMI)和2,6,10,15,19,23-六甲基二十四烷(Squalane-Sq角鲨烷)的13C亏损强烈(δ13C值介于-74.2‰~-119.0‰PDB之间),表明碳酸盐岩形成于AOM,同时反映该研究区曾发生过强烈、持续的富CH₄流体释放活动.柱状泥质沉积物中,AOM生物标志化合物在硫酸岩-甲烷过渡带(SMI-Sulfate-Methane Interface)边界附近相对丰度高,SMI之上样品中含量低,或未检出,表明现代环境在SMI附近有大量嗜甲烷微生物生长,使得深部上升的甲烷被大量消耗,很少有甲烷逸出海底.AOM生物标志化合物可用来指示SMI边界.不同站位、不同岩性AOM生物标志化合物组成(包括碳同位素组成)的差异反映了嗜甲烷古细菌组成的不同.  相似文献   

Nitrification in Kochi backwaters     

Joereen Miranda  K.K. Balachandran  R. Ramesh  Mohideen Wafar 《Estuarine, Coastal and Shelf Science》2008

Nitrification rates, as oxidation of ¹⁵N-labelled ammonium and loss of nitrite from N-Serve treated samples, were measured in Kochi backwaters during three seasons. Nitrification rates ranged from undetectable to 166 nmol N L⁻¹ h⁻¹ in the water column and up to 17 nmol N (g wet wt)⁻¹ h⁻¹ in sediments. Nitrification rates were higher in intermediate salinities than in either freshwater or seawater end. Within this salinity range, nitrification rates could be related to ammonium concentrations. As shown by the relation between ammonification and nitrification rates, it is also likely that nitrification is more regulated by renewal rates, rather than by in situ concentrations, of substrate. Among other environmental parameters, temperature and pH may have an influence on nitrification. Potential nitrification rates calculated from loss of nitrite from N-Serve treated, nitrite-enriched samples were about 800 nmol N L⁻¹ h⁻¹ in the water column and 40 nmol N (g wet wt)⁻¹ h⁻¹ in sediments. While these rates are in balance with those of biological ammonium production they may be inadequate to mitigate ammonium pollution in this estuary.  相似文献